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2009480
17-Hydroxyprogesterone 60-Min Quantitative by HPLC-MS/MS, Serum or Plasma
OHPRGSTN60
Ordering Recommendation
New York DOH Approval Status
This test is New York state approved.
Specimen Required
Patient Preparation
Collect
Serum separator tube. Also acceptable: Plain red, pink (K2EDTA), plasma separator tube, green (sodium heparin), or green (lithium heparin).
Specimen Preparation
Transfer 1 mL serum or plasma to an ARUP standard transport tube. (Min: 0.3 mL)
Storage/Transport Temperature
Refrigerated. Also acceptable: Frozen.
Unacceptable Conditions
Grossly hemolyzed specimens.
Remarks
Stability
After separation from cells: Ambient: Unacceptable; Refrigerated: 1 week; Frozen: 6 months
Methodology
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed
Sun-Sat
Reported
1-5 days
Reference Interval
Interpretive Data
Reference ranges for 17-hydroxyprogesterone following stimulation are not well defined and are dependent on the stimulation method utilized.
Compliance Category
Laboratory Developed Test (LDT)
Note
Hotline History
Hotline History
Date of Change
Test Name Change
Methodology
Performance/Reported Schedule
Specimen Requirements
Reference Interval
Interpretive Data
Note
CPT Code
Component Change
Other Interface Change
New Test
Inactive
N/A
CPT Codes
83498
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 2009481 | 17-Hydroxyprogesterone 60min, HPLC-MS/MS | 48341-2 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
17-Hydroxyprogesterone 60-Min Quantitative by HPLC-MS/MS, Serum or Plasma
